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Sklar®
SKLAR CORPORATION · Model 48-904 · UDI-DI 10649111007118
10
510(k) clearances
11
Adverse events
1
Recalls
215
Facilities
Description
STANDARD EXTRACTING FORCEPS #1
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-05-21 | Biomet Microfixation, Inc. | The Biomet Microfixation Obwegeser Ramus Clamp, Wide Right 01-7996 were incorrectly etched as the left part number 01-7997. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.